Canonical Allele Identifier: PA2828733049
Gene: SPAST HGNC NCBI

Linked Data

ClinVar Variation Id: 5672

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364888.1:p.Pro45Gln
CA117671
NM_001377959.1:c.134C>A